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Meicet

FDA UDI

Class II (US FDA UDI)

by Shanghai May Skin Information Technology Co., Ltd.

Identity

Trade Name
MEICET FDA UDI
Generic Name
Liquid-jet skin surface treatment system control unit FDA UDI
Model / Reference
MC-A2 FDA UDI

Identifiers

Primary DI / UDI-DI
06975980571007 FDA UDI
FDA Product Code
MQX FDA UDI
GMDN Term
Liquid-jet skin surface treatment system control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5580 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Liquid-jet skin surface treatment system control unit

Meicet by Shanghai May Skin Information Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liquid-jet skin surface treatment system control unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shanghai May Skin Information Technology Co., Ltd.

Sources (1)

  • FDA UDI 449bae11-19a4-4548-8c53-50f534aeff0d 32 fields · synced Jun 7, 2026